These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

217 related articles for article (PubMed ID: 12700168)

  • 1. Transgenic expression of a dominant-negative connexin26 causes degeneration of the organ of Corti and non-syndromic deafness.
    Kudo T; Kure S; Ikeda K; Xia AP; Katori Y; Suzuki M; Kojima K; Ichinohe A; Suzuki Y; Aoki Y; Kobayashi T; Matsubara Y
    Hum Mol Genet; 2003 May; 12(9):995-1004. PubMed ID: 12700168
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Cochlear outer hair cells in a dominant-negative connexin26 mutant mouse preserve non-linear capacitance in spite of impaired distortion product otoacoustic emission.
    Minekawa A; Abe T; Inoshita A; Iizuka T; Kakehata S; Narui Y; Koike T; Kamiya K; Okamura HO; Shinkawa H; Ikeda K
    Neuroscience; 2009 Dec; 164(3):1312-9. PubMed ID: 19712724
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Postnatal development of the organ of Corti in dominant-negative Gjb2 transgenic mice.
    Inoshita A; Iizuka T; Okamura HO; Minekawa A; Kojima K; Furukawa M; Kusunoki T; Ikeda K
    Neuroscience; 2008 Oct; 156(4):1039-47. PubMed ID: 18793701
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Timed conditional null of connexin26 in mice reveals temporary requirements of connexin26 in key cochlear developmental events before the onset of hearing.
    Chang Q; Tang W; Kim Y; Lin X
    Neurobiol Dis; 2015 Jan; 73():418-27. PubMed ID: 25251605
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Virally expressed connexin26 restores gap junction function in the cochlea of conditional Gjb2 knockout mice.
    Yu Q; Wang Y; Chang Q; Wang J; Gong S; Li H; Lin X
    Gene Ther; 2014 Jan; 21(1):71-80. PubMed ID: 24225640
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Down regulated connexin26 at different postnatal stage displayed different types of cellular degeneration and formation of organ of Corti.
    Chen S; Sun Y; Lin X; Kong W
    Biochem Biophys Res Commun; 2014 Feb; 445(1):71-7. PubMed ID: 24491564
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The human deafness-associated connexin 30 T5M mutation causes mild hearing loss and reduces biochemical coupling among cochlear non-sensory cells in knock-in mice.
    Schütz M; Scimemi P; Majumder P; De Siati RD; Crispino G; Rodriguez L; Bortolozzi M; Santarelli R; Seydel A; Sonntag S; Ingham N; Steel KP; Willecke K; Mammano F
    Hum Mol Genet; 2010 Dec; 19(24):4759-73. PubMed ID: 20858605
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A deafness mechanism of digenic Cx26 (GJB2) and Cx30 (GJB6) mutations: Reduction of endocochlear potential by impairment of heterogeneous gap junctional function in the cochlear lateral wall.
    Mei L; Chen J; Zong L; Zhu Y; Liang C; Jones RO; Zhao HB
    Neurobiol Dis; 2017 Dec; 108():195-203. PubMed ID: 28823936
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular genetics of hearing impairment due to mutations in gap junction genes encoding beta connexins.
    Rabionet R; Gasparini P; Estivill X
    Hum Mutat; 2000 Sep; 16(3):190-202. PubMed ID: 10980526
    [TBL] [Abstract][Full Text] [Related]  

  • 10. BAAV mediated GJB2 gene transfer restores gap junction coupling in cochlear organotypic cultures from deaf Cx26Sox10Cre mice.
    Crispino G; Di Pasquale G; Scimemi P; Rodriguez L; Galindo Ramirez F; De Siati RD; Santarelli RM; Arslan E; Bortolozzi M; Chiorini JA; Mammano F
    PLoS One; 2011; 6(8):e23279. PubMed ID: 21876744
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Developmental abnormalities in supporting cell phalangeal processes and cytoskeleton in the
    Chen S; Xie L; Xu K; Cao HY; Wu X; Xu XX; Sun Y; Kong WJ
    Dis Model Mech; 2018 Feb; 11(2):. PubMed ID: 29361521
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Dominant negative connexin26 mutation R75W causing severe hearing loss influences normal programmed cell death in postnatal organ of Corti.
    Inoshita A; Karasawa K; Funakubo M; Miwa A; Ikeda K; Kamiya K
    BMC Genet; 2014 Jan; 15():1. PubMed ID: 24387126
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Connexins, hearing and deafness: clinical aspects of mutations in the connexin 26 gene.
    Lefebvre PP; Van De Water TR
    Brain Res Brain Res Rev; 2000 Apr; 32(1):159-62. PubMed ID: 10928803
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Deficiency of transcription factor Brn4 disrupts cochlear gap junction plaques in a model of DFN3 non-syndromic deafness.
    Kidokoro Y; Karasawa K; Minowa O; Sugitani Y; Noda T; Ikeda K; Kamiya K
    PLoS One; 2014; 9(9):e108216. PubMed ID: 25259580
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Reduced postnatal expression of cochlear Connexin26 induces hearing loss and affects the developmental status of pillar cells in a dose-dependent manner.
    Xie L; Chen S; Xu K; Cao HY; Du AN; Bai X; Sun Y; Kong WJ
    Neurochem Int; 2019 Sep; 128():196-205. PubMed ID: 31034913
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Targeted connexin26 ablation arrests postnatal development of the organ of Corti.
    Wang Y; Chang Q; Tang W; Sun Y; Zhou B; Li H; Lin X
    Biochem Biophys Res Commun; 2009 Jul; 385(1):33-7. PubMed ID: 19433060
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Connexin32 can restore hearing in connexin26 deficient mice.
    Degen J; Schütz M; Dicke N; Strenzke N; Jokwitz M; Moser T; Willecke K
    Eur J Cell Biol; 2011 Oct; 90(10):817-24. PubMed ID: 21813206
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel missense mutation in the second extracellular domain of GJB2, p.Ser183Phe, causes a syndrome of focal palmoplantar keratoderma with deafness.
    de Zwart-Storm EA; van Geel M; van Neer PA; Steijlen PM; Martin PE; van Steensel MA
    Am J Pathol; 2008 Oct; 173(4):1113-9. PubMed ID: 18787097
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cell degeneration is not a primary causer for Connexin26 (GJB2) deficiency associated hearing loss.
    Liang C; Zhu Y; Zong L; Lu GJ; Zhao HB
    Neurosci Lett; 2012 Oct; 528(1):36-41. PubMed ID: 22975134
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Connexin 26 null mice exhibit spiral ganglion degeneration that can be blocked by BDNF gene therapy.
    Takada Y; Beyer LA; Swiderski DL; O'Neal AL; Prieskorn DM; Shivatzki S; Avraham KB; Raphael Y
    Hear Res; 2014 Mar; 309():124-35. PubMed ID: 24333301
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.